CN101641419A - Adhesive for optical film and adhesive optical film - Google Patents

Adhesive for optical film and adhesive optical film Download PDF

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Publication number
CN101641419A
CN101641419A CN200880007229A CN200880007229A CN101641419A CN 101641419 A CN101641419 A CN 101641419A CN 200880007229 A CN200880007229 A CN 200880007229A CN 200880007229 A CN200880007229 A CN 200880007229A CN 101641419 A CN101641419 A CN 101641419A
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acrylic copolymer
condition
weight
methyl
sensitive adhesive
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CN200880007229A
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CN101641419B (en
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近藤真
中泽光彦
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Soken Kagaku KK
Soken Chemical and Engineering Co Ltd
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Soken Chemical and Engineering Co Ltd
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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C09J133/04—Homopolymers or copolymers of esters
    • C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09J133/062—Copolymers with monomers not covered by C09J133/06
    • C09J133/066—Copolymers with monomers not covered by C09J133/06 containing -OH groups
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
    • C09J7/38—Pressure-sensitive adhesives [PSA]
    • C09J7/381—Pressure-sensitive adhesives [PSA] based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C09J7/385—Acrylic polymers
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00—Optical elements other than lenses
    • G02B5/30—Polarising elements
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2433/00—Presence of (meth)acrylic polymer
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
    • Y10T428/2852—Adhesive compositions
    • Y10T428/2878—Adhesive compositions including addition polymer from unsaturated monomer
    • Y10T428/2887—Adhesive compositions including addition polymer from unsaturated monomer including nitrogen containing polymer [e.g., polyacrylonitrile, polymethacrylonitrile, etc.]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
    • Y10T428/2852—Adhesive compositions
    • Y10T428/2878—Adhesive compositions including addition polymer from unsaturated monomer
    • Y10T428/2891—Adhesive compositions including addition polymer from unsaturated monomer including addition polymer from alpha-beta unsaturated carboxylic acid [e.g., acrylic acid, methacrylic acid, etc.] Or derivative thereof

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Adhesive Tapes (AREA)
  • Polarising Elements (AREA)
  • Laminated Bodies (AREA)

Abstract

Disclosed is an acrylic adhesive for optical films, which is excellent in elastic balance and optical characteristics. Also disclosed is an optical film processed to be adhesive. Specifically disclosed is an adhesive for optical films, which satisfies specific conditions and contains an acrylic copolymer (A) which is obtained by copolymerizing 95.0-98.0 parts by weight of an n-butyl acrylate (a),2.0-5.0 parts by weight of a hydroxyl group-containing (meth)acrylate (b) represented by the general formula (1) below, and not more than 2.0 parts by weight of a (meth)acrylic acid (c) (with the total of (a)-(c) being 100 parts by weight).

Description

Pressure-sensitive adhesive for optical films and bonding processing optical film
Technical field
The present invention relates to pressure-sensitive adhesive for optical films and bonding processing optical film, be specifically related to comprise the pressure-sensitive adhesive for optical films of specific acrylic polymers and adopt the bonding processing optical film of this tackiness agent.
Background technology
In slim display unit such as liquid-crystal display, plasma display, need to use tackiness agent to attach the film of as polarizer, polaroid etc., giving specific function.Slim display unit so constantly maximizes in recent years, and for its environment for use, also uses under the such exacting terms of for example onboard navigation system more and more.The environment for use of such thin-type display device is more and more harsher, and along with the maximization of display unit, in the functional membrane of such employing tackiness agent, peeling off, swell etc. of binder layer is taken place more and more easily.
In order to prevent peeling off, swell etc. of such binder layer, 1000% modulus that for example must make the acrylic copolymer that forms tackiness agent is in certain scope, and the tensile properties of this acrylic copolymer is good.Characteristics such as breaking tenacity when in addition, applying tensile stress certainly must be good.Yet, if actual trial-production tackiness agent, can find that then the good tackiness agent of the balance of all such characteristics is few, because such balance of properties is not good, so to be some characteristic mostly good and the balanced differences of characteristic on the whole for tackiness agent, good and the poor heat resistance of humidity resistance for example, perhaps opposite good heat resistance and humidity resistance difference etc.
Under the little situation of the area of the display part of the good and display unit of the environment for use of display unit,, also seldom can produce directly influence because of the uneven characteristic of such characteristic to display unit even the balance of characteristic is poor slightly.Yet for display unit of using under exacting terms and the display unit that surpasses 100 inches big picture, small characteristic is unbalance also can be easy to the form that the characteristic with display unit descends and to display.Specifically, balance of properties not good shows as peeling off, swelling of cling film under the heated condition and the generation that swells, peels off when using under the high condition of humidity and temperature.
Therefore, for employed tackiness agent in the aforesaid display unit, the balance of characteristic is very important.
In addition, as employed tackiness agent in the aforesaid display unit, extensively adopt the tackiness agent that forms by acrylic resin.The tackiness agent that is formed by acrylic resin is like this gone up substantially by following method manufacturing: (methyl) vinylformic acid reaction that makes (methyl) acrylate of (methyl) alkyl acrylate, polar functionalities and adopt as required, and in the multipolymer of gained, mix as bridging property composition such as isocyanate compound and form crosslinking structure with certain cross-linking density.As (methyl) acrylate of employed polar functionalities here, in order to form good crosslinking structure by isocyanate compound as linking agent, make tackiness agent self form three-dimensional crosslinking structure, thereby prevent to adopt (methyl) acrylic compounds of hydroxyl mostly as the dislocation (Japanese: ず れ Write body) on the molecular level of the acrylic copolymer of macromolecular compound.In addition, a spot of by making (methyl) acrylic acid copolymer just can be used as whole higher elongation, breaking tenacity, 1000% modulus that keep.
For employed tackiness agent in display unit like this, the composition of copolymer composition is determined basically, the balance that is considered to its characteristic also presents stable value in certain scope, it is generally acknowledged that the technology of the tackiness agent of display unit has reached perfect substantially degree.
Therefore, the peeling off of the functional membrane when using under utmost point exacting terms, foaming etc. are considered to take place with certain probability, can't prevent its generation fully.In addition, though be exacting terms, it also is the interior exacting terms of temperature range of liquid crystal drive, peel off or the generation of foaming etc. even under the condition that liquid crystal does not drive, have slightly, if be exactly the condition that liquid crystal does not drive originally, do not think that so the discussion of characteristics such as peeling off, swell of the tackiness agent under such condition itself has great meaning yet.
But, most life-time service such as the display unit of liquid crystal etc., reach tens thousand of hours duration of service, infers that the small decline of characteristic constantly adds up in such life-time service, and shorten the work-ing life of final display unit.For such display unit, the degradation of part of bearing the keying action of display unit because of the deterioration of liquid crystal material, the degradation of plasma body etc. becomes display unit can't drive the mechanical life that is considered to this display unit, and the function reduction of the display unit that causes such as peeling off, swell of the functional membrane that it is peripheral is the problem that should not occur as display unit.
If come employed tackiness agent the display unit is tried to study in more detail, then find there is the tackiness agent of the faster deterioration of part of bearing the keying action of display unit than liquid crystal etc. from such viewpoint.Therefore, such tackiness agent also has further room for improvement.
For example, following example shown in the comparative example 2 of the comparative example 3 of patent documentation 1 (Japanese patent laid-open 10-44293 communique) and patent documentation 2 (Japanese patent laid-open 10-44294 communique): use 94.9 parts by weight of acrylic acid butyl esters, 5 parts by weight of acrylic acid and 0.1 parts by weight of acrylic acid-2-hydroxy methacrylate to make the acrylic polymers of molecular-weight average 1,550,000 as monomer, in the solution of described acrylic polymers, add 1.2 weight part TriMethylolPropane(TMP) tolylene diisocyanates, use formed acrylic adhesives to make blooming.Yet when adopting aforesaid composition, 1000% modulus is 16g/mm 2Or 30g/mm 2, but elongation at break is 700%, the elongation deficiency.In addition, about optical characteristics, also put down in writing the decline of the degree of polarization of finding to influence identification on the whole, so be judged as the tackiness agent that is not suitable as blooming.
When making acrylic polymers like this, known (methyl) acrylic ester copolymer that makes n-butyl acrylate, (methyl) vinylformic acid, hydroxyl.Yet, the multipolymer that forms even use these monomers, characteristics such as elongation, breaking tenacity, 1000% modulus are also significantly different according to using monomeric amount, polymerization state etc., can't obtain the good polymkeric substance of balance of these characteristics.
In addition, in patent documentation 3 (the Japanese Patent spy opens clear 59-111115 communique), patent documentation 4 (Japanese patent laid-open 3-12471 communique), patent documentation 5 (Japanese patent laid-open 2-194081 communique), patent documentation 6 (the Japanese Patent spy opens the 2004-91500 communique), patent documentation 7 all kinds of communiques such as (the Japanese Patent spy open the 2005-196006 communique) relevant for the record of the tackiness agent of bonding optical component or caking agent etc.Yet tackiness agent of being put down in writing in these communiques or caking agent have problems aspect elasticity, and tackiness agent or caking agent can't be complied with base material under exacting terms, may cause peeling off or foaming.
The display unit of liquid crystal etc. is used under its purposes high temperature that also imagination is good wets condition more sometimes, must also can stably use under such severe condition.Constitute in the member of such display unit, tackiness agent or caking agent are subjected to the influence of temperature or humidity generation easily, may peel off because of the thermal distortion of tackiness agent etc. by functional optical films such as bonding polaroid of such tackiness agent or caking agent or polarizers, the binder layer foaming perhaps takes place and lose the situation of its function.
Patent documentation 1: Japanese patent laid-open 10-44293 communique
Patent documentation 2: Japanese patent laid-open 10-44294 communique
Patent documentation 3: the Japanese Patent spy opens clear 59-111115 communique
Patent documentation 4: Japanese patent laid-open 3-12471 communique
Patent documentation 5: Japanese patent laid-open 2-194081 communique
Patent documentation 6: the Japanese Patent spy opens the 2004-91500 communique
Patent documentation 7: the Japanese Patent spy opens the 2005-196006 communique
The announcement of invention
Useful novel optical film is with tackiness agent and adopt the bonding processing optical film of this tackiness agent when the object of the present invention is to provide in attaching liquid crystal indicator etc. employed functional optical film.
Purpose of the present invention particularly is to provide thermotolerance and the good tackiness agent of humidity resistance.
The inventor is conscientiously research back discovery repeatedly in order to solve above-mentioned problem, and the pressure-sensitive adhesive for optical films that comprises specific acrylic polymers is very useful when attaching the functional optical film, thereby has finished the present invention.
Pressure-sensitive adhesive for optical films of the present invention be comprise with (a) n-butyl acrylate 95.0～98.0 weight parts, (b) with (methyl) acrylate 2.0～5.0 weight parts of the hydroxyl of following formula (1) expression and (c) the following amount copolymerization of (methyl) vinylformic acid 2.0 weight parts and (A) acrylic copolymer, and satisfy the pressure-sensitive adhesive for optical films of following condition (1)～(3), the summation of above-mentioned (a)～(c) is 100 weight parts;
Condition (1): (A) acrylic copolymer passes through weight-average molecular weight that polystyrene standard that gel permeation chromatography records converts in 1,300,000～2,000,000 scope;
Condition (2): (A) acrylic copolymer in being dissolved in organic solvent adds (B-1) linking agent, the condition that reaches 1mm with dried thickness is coated on the separability PET film, form coating layer, by drying remove desolvate after, lining separability PET film on the another side of this coating layer, slaking is 4～7 days under 23 ℃, the condition of 65%RH, from the adhesive sheet of gained with 5mm * 30mm * 1mm tSize cut out sample, the elongation in the times of try to achieve when using described sample 90 ℃ is at (2-1) more than 1400%, the breaking tenacity in the time of 90 ℃ is at 13～30g/mm 2Scope in (2-2), and 1000% modulus 90 ℃ the time is at 10～20g/mm 2Scope in (2-3);
Condition (3): the gel fraction of described adhesive sheet is in 65～95% scope;
Figure G2008800072290D00051
In the above-mentioned formula (1), R 1Expression hydrogen atom or methyl, R 2The alkyl of expression hydrogen atom or carbon number 1～2.
Pressure-sensitive adhesive for optical films of the present invention can be comprise with (a) n-butyl acrylate 95.0～98.0 weight parts, (b) with (methyl) acrylate 2.0～5.0 weight parts of the hydroxyl of following formula (1) expression and (c) the following amount copolymerization of (methyl) vinylformic acid 2.0 weight parts and (A) acrylic copolymer and (B-2) linking agent, and satisfy the pressure-sensitive adhesive for optical films of following condition (1)～(3), the summation of above-mentioned (a)～(c) is 100 weight parts;
Condition (1): (A) acrylic copolymer passes through weight-average molecular weight that polystyrene standard that gel permeation chromatography records converts in 1,300,000～2,000,000 scope;
Condition (2): (A) acrylic copolymer in being dissolved in organic solvent adds (B-1) linking agent, the condition that reaches 1mm with dried thickness is coated on the separability PET film, form coating layer, by drying remove desolvate after, lining separability PET film on the another side of this coating layer, slaking is 4～7 days under 23 ℃, the condition of 65%RH, cut out sample from the adhesive sheet of gained with the size of 5mm * 30mm * 1mm, elongation in the times of try to achieve when using described sample 90 ℃ is at (2-1) more than 1400%, and the breaking tenacity in the time of 90 ℃ is at 13～30g/mm 2Scope in (2-2), and 1000% modulus 90 ℃ the time is at 10～20g/mm 2Scope in (2-3);
Condition (3): the gel fraction of described adhesive sheet is in 65～95% scope;
Figure G2008800072290D00061
In the above-mentioned formula (1), R 1Expression hydrogen atom or methyl, R 2The alkyl of expression hydrogen atom or carbon number 1～2.
Better be in the described condition (2), if (A) acrylic copolymer is made as 100 weight parts, then (B-1) linking agent is 0.1～0.4 weight part.
Better be that then (B-2) linking agent is 0.1～0.4 weight part if contained in the described pressure-sensitive adhesive for optical films (A) acrylic copolymer is made as 100 weight parts.
Better be that described (B-1) linking agent is an isocyanate compound.
Better be that described (B-2) linking agent is an isocyanate compound.
Better be that described (A) acrylic copolymer is a terpolymer.
The part of described (a) n-butyl acrylate can be replaced by (methyl) alkyl acrylate except that n-butyl acrylate.
The present invention includes bonding processing optical film, it is characterized in that, comprise functional optical film and the binder layer that on the functional optical film, forms by following pressure-sensitive adhesive for optical films;
Described pressure-sensitive adhesive for optical films comprise with (a) n-butyl acrylate 95.0～98.0 weight parts, (b) with (methyl) acrylate 2.0～5.0 weight parts of the hydroxyl of following formula (1) expression and (c) the following amount copolymerization of (methyl) vinylformic acid 2.0 weight parts and (A) acrylic copolymer and (B-2) linking agent, and satisfy following condition (1)～(3), the summation of above-mentioned (a)～(c) is 100 weight parts;
Condition (1): (A) acrylic copolymer passes through weight-average molecular weight that polystyrene standard that gel permeation chromatography records converts in 1,300,000～2,000,000 scope;
Condition (2): (A) acrylic copolymer in being dissolved in organic solvent adds (B-1) linking agent, the condition that reaches 1mm with dried thickness is coated on the separability PET film, form coating layer, by drying remove desolvate after, lining separability PET film on the another side of this coating layer, slaking is 4～7 days under 23 ℃, the condition of 65%RH, cut out sample from the adhesive sheet of gained with the size of 5mm * 30mm * 1mm, elongation in the times of try to achieve when using described sample 90 ℃ is at (2-1) more than 1400%, and the breaking tenacity in the time of 90 ℃ is at 13～30g/mm 2Scope in (2-2), and 1000% modulus 90 ℃ the time is at 10～20g/mm 2Scope in (2-3);
Condition (3): the gel fraction of described adhesive sheet is in 65～95% scope;
Figure G2008800072290D00071
In the above-mentioned formula (1), R 1Expression hydrogen atom or methyl, R 2The alkyl of expression hydrogen atom or carbon number 1～2.
The main origin of main chain of contained (A) acrylic copolymer comes from the formation unit formation of n-butyl acrylate in the pressure-sensitive adhesive for optical films of the present invention, is somebody's turn to do the side chain with following formula (X) expression that (A) acrylic copolymer has (methyl) acrylate that derives from the hydroxyl of representing with above-mentioned formula (1).
Figure G2008800072290D00072
In the above-mentioned formula (X), R 2The alkyl of expression hydrogen atom or carbon number 1～2.In addition, Y represents and the combining of main chain.
The main chain of (A) acrylic copolymer that uses among the present invention has owing to the side chain with above-mentioned formula (X) expression is difficult for closely approaching structure mutually.Derive from formation unit with (methyl) acrylate of the hydroxyl of above-mentioned formula (1) expression and have side chain with above-mentioned formula (X) expression, contained hydroxyl is the reflecting point with the linking agent (isocyanate compound) that forms crosslinking structure in this side chain.
During by linking agent (isocyanate compound) crosslink propylene acid copolymer, cross-linking set has tremendous influence with respect to the position of main chain to the characteristic through crosslinked acrylic copolymer of gained.That is, required power is little if cross-linking set, then demonstrates 1000% elongation away from the main chain of acrylic copolymer, but elongation is low, for the breaking tenacity of this acrylic copolymer, the quantity of the atom of participation crosslinking structure is many more simultaneously, and the intensity when then rupturing is low more.
And, above-mentioned by using (A) acrylic copolymer, the elongation that can make characteristic essential when being used for that functional membrane is attached at display unit is more than 1400%, and breaking tenacity is at 13～30g/mm 2Scope in, 1000% modulus is at 10～20g/mm 2Scope in.
Pressure-sensitive adhesive for optical films of the present invention comprises (A) acrylic copolymer, (A) acrylic copolymer has the side chain of above-mentioned formula (X) expression, and the hydroxyl that this side chain had becomes the reflecting point that uses the crosslinking structure that linking agent (isocyanate compound) forms.That is, (A) second carbon atom bonded hydroxyl with begin number from-CO-O-base of the side chain of acrylic copolymer becomes the reflecting point that uses the crosslinking structure that linking agent (isocyanate compound) forms.In addition, the side chain that (A) has the alkyl that derives from (a) n-butyl acrylate in a large number in the acrylic copolymer with carbon number 4.
Therefore, in (A) acrylic copolymer, formed crosslinking structure even use linking agent (isocyanate compound), also there is the side chain that derives from (a) n-butyl acrylate in a large number around the main chain, (A) may approach to the distance suitable between the main chain of acrylic copolymer, but further approaching possibility is very little with the length of this side chain.Therefore, the molecule of acrylic copolymer itself does not tangle mutually, can relatively move smoothly, so elongation improves, but because the side chain by will (A) acrylic copolymer with begin second several carbon atom bonded hydroxyls to react from-CO-O-base as starting point and linking agent (isocyanate compound) in intermolecular formation crosslinking structure, even so the tensile stress of applying, formed crosslinking structure also can play the effect of the sliding phenomenon that suppresses molecule.
In addition, in (c) (methyl) vinylformic acid as the 3rd copolymer composition, the carboxyl that forms side chain exists in the mode that is imbedded in the side chain that is arranged in (a) n-butyl acrylate on every side, the carboxyl that participates in crosslinking structure formation is few, mostly keep such structure and be present in (A) acrylic copolymer after crosslinked, most of the binding property of pressure-sensitive adhesive for optical films is made contributions.
If adopt pressure-sensitive adhesive for optical films of the present invention like this, then, therefore can give play to good characteristic owing to comprise specific (A) acrylic polymers.
For example, when using vinylformic acid-positive butyl ester of 4-hydroxyl to replace (b) with (methyl) acrylate of the hydroxyl of formula (1) expression, the start point distance of crosslinking structure is far away excessively from main chain, therefore can't bring into play aforesaid characteristic.
The best mode that carries out an invention
Below, to pressure-sensitive adhesive for optical films of the present invention and adopt the bonding processing optical film of this tackiness agent to be specifically described.
Pressure-sensitive adhesive for optical films of the present invention be comprise with (a) n-butyl acrylate 95.0～98.0 weight parts, (b) with (methyl) acrylate 2.0～5.0 weight parts of the hydroxyl of following formula (1) expression and (c) the following amount copolymerization of (methyl) vinylformic acid 2.0 weight parts and (A) acrylic copolymer, better be also to comprise (B-2) linking agent, and satisfy the pressure-sensitive adhesive for optical films of following condition (1)～(3), the summation of above-mentioned (a)～(c) is 100 weight parts;
Condition (1): (A) acrylic copolymer passes through weight-average molecular weight that polystyrene standard that gel permeation chromatography records converts in 1,300,000～2,000,000 scope;
Condition (2): (A) acrylic copolymer in being dissolved in organic solvent adds (B-1) linking agent, the condition that reaches 1mm with dried thickness is coated on the separability PET film, form coating layer, by drying remove desolvate after, lining separability PET film on the another side of this coating layer, slaking is 4～7 days under 23 ℃, the condition of 65%RH, cut out sample from the adhesive sheet of gained with the size of 5mm * 30mm * 1mm, elongation in the times of try to achieve when using described sample 90 ℃ is at (2-1) more than 1400%, and the breaking tenacity in the time of 90 ℃ is at 13～30g/mm 2Scope in (2-2), and 1000% modulus 90 ℃ the time is at 10～20g/mm 2Scope in (2-3);
Condition (3): the gel fraction of described adhesive sheet is in 65～95% scope;
In the above-mentioned formula (1), R 1Expression hydrogen atom or methyl, R 2The alkyl of expression hydrogen atom or carbon number 1～2.
Comprise in used (A) acrylic copolymer in the pressure-sensitive adhesive for optical films of the present invention by (a) n-butyl acrylate deutero-constitute the unit, by (b) with (methyl) acrylate deutero-of the hydroxyl of above-mentioned formula (1) expression constitute the unit and adopt as required derive from the acrylic acid formation of (c) (methyl) unit.
Also have, (A) in the acrylic copolymer, the part of above-mentioned (a) n-butyl acrylate can be replaced by other (methyl) alkyl acrylates.Among the present invention, as the example of (methyl) alkyl acrylate that uses with (a) n-butyl acrylate, carbon number that can exemplified by alkyl groups is (methyl) alkyl acrylate of 1～18 (but not comprising normal-butyl); As preferred example, can exemplify (methyl) methyl acrylate, (methyl) ethyl propenoate, (methyl) vinylformic acid n-propyl, (methyl) isopropyl acrylate, (methyl) isobutyl acrylate, (methyl) tert-butyl acrylate, (methyl) Isooctyl acrylate monomer, (methyl) vinylformic acid pentyl ester, (methyl) Ethyl acrylate, (methyl) vinylformic acid heptyl ester, (methyl) Octyl acrylate, (methyl) vinylformic acid ester in the ninth of the ten Heavenly Stems, (methyl) decyl acrylate, (methyl) vinylformic acid undecyl ester, (methyl) dodecylacrylate, (methyl) tridecyl acrylate, (methyl) vinylformic acid tetradecyl ester, (methyl) vinylformic acid pentadecyl ester, (methyl) vinylformic acid cetyl ester, (methyl) vinylformic acid heptadecyl ester and (methyl) vinylformic acid stearyl, (methyl) ethyl acrylate etc.
When the usage quantity of employed (a) n-butyl acrylate was made as 100 weight parts, the usage quantity of such other (methyl) alkyl acrylate usually can be at 0～40 weight part, better be in the scope of 0～30 weight part.That is, even with aforesaid amount use (methyl) alkyl acrylate except that n-butyl acrylate, the good action effect in the time of also can not making whole uses (a) n-butyl acrylate significantly descends.In addition,, there is add-on corresponding to (methyl) methyl acrylate by also usefulness (methyl) methyl acrylate and (a) n-butyl acrylate, the acrylic copolymer hardening, elongation and breaking tenacity demonstrate the tendency of higher value.Under this situation, if will (a) n-butyl acrylate and total usage quantity of (methyl) methyl acrylate be made as 100 weight parts, then n-butyl acrylate and (methyl) methyl acrylate usually with in 9: 1～6: 4 the scope, better be weight ratio use in 8: 2～7: 3 the scope.
Constitute in (A) acrylic copolymer of pressure-sensitive adhesive for optical films of the present invention, except (a) n-butyl acrylate, also copolymerization has (b) (methyl) acrylate with the hydroxyl of following formula (1) expression.
Figure G2008800072290D00111
In the above-mentioned formula (1), R 1Expression hydrogen atom or methyl, R 2The alkyl of expression hydrogen atom or carbon number 1～2.
In the above-mentioned formula (1), R 2For the compound of hydrogen atom is (methyl) 2-Hydroxy ethyl acrylate (following formula (1-1)), R 2For the compound of methyl is (methyl) vinylformic acid-2-hydroxy propyl ester (following formula (2)), R 2For the compound of ethyl is (methyl) vinylformic acid-2-hydroxyl butyl ester (following formula (3)).
Figure G2008800072290D00112
In above-mentioned formula (1-1), (2), (3), R 1Expression hydrogen atom or methyl.
Shown in above-mentioned structural formula, employed among the present invention (b) is shown in above-mentioned formula (1-1), (2), (3) with (methyl) acrylate of the hydroxyl of above-mentioned formula (1) expression, with (methyl) acrylate that is combined with hydroxyl on carbon atom (I) the bonded carbon atom (carbon atom of representing with (II) in above-mentioned formula (1-1), (2), (3)).
(methyl) hydroxyl that acrylate had of such hydroxyl with as the reaction of the isocyanate compound of linking agent, mainly at intermolecular formation linking agent, the mutual alignment relation of the molecule of restriction acrylic copolymer.Constitute in the acrylic copolymer of pressure-sensitive adhesive for optical films of the present invention, as the isocyanate compound bonded binding site of linking agent be acrylic copolymer side chain with begin second carbon atom bonded hydroxyl of number from-CO-O-base.This position is positioned at the position of the more close main chain side of front end that ratio based on monomeric (A) acrylic copolymer of n-butyl acrylate derives from the side chain of n-butyl acrylate.
By existing the hydroxyl of specific distance to come the crosslink propylene acid copolymer with the main chain of (A) acrylic copolymer like this, can make being equilibrated in the scope that is suitable as the tackiness agent that is used to attach blooming of elongation, breaking tenacity and 1000% modulus of tackiness agent as cross-linking set.
Relative with it, acrylic compounds as hydroxyl, when for example adopting the compound with following formula (4) expression, from with polymerizability double linked-the CO-O-base begin the number four carbon atom be combined with hydroxyl, have the acrylic compounds of hydroxyl even use like this in position away from the two keys of polymerizability, also can overbalance as the drawing force and the intensity of the tackiness agent that is used to attach blooming.
Figure G2008800072290D00121
In the above-mentioned formula (4), R 1Expression hydrogen atom or methyl.
Constitute in the acrylic copolymer of pressure-sensitive adhesive for optical films of the present invention, except above-mentioned (a) n-butyl acrylate, (b) (methyl) acrylate, can also (c) (methyl) vinylformic acid be arranged copolymerization with the hydroxyl of formula (1) expression.
(methyl) vinylformic acid is shown in following formula (5).
Figure G2008800072290D00122
In the above-mentioned formula (5), R 1Expression hydrogen atom or methyl.
(A) acrylic copolymer that uses among the present invention forms with (methyl) acrylic ester copolymer of the hydroxyl of above-mentioned formula (1) expression by (a) n-butyl acrylate with (b), and also copolymerization has (c) (methyl) vinylformic acid.(A) of the present invention acrylic copolymer have at least with formula (7-1) and (7-2) 2 kinds of expression constitute unit, 3 kinds that can have with formula (7-1)～(7-3) expression become subdivisions.
Figure G2008800072290D00131
In the above-mentioned formula (7), R 1Represent hydrogen atom or methyl, R respectively independently 2The alkyl of expression hydrogen atom or carbon number 1～2.
(A) acrylic copolymer that constitutes pressure-sensitive adhesive for optical films of the present invention is by using (a) n-butyl acrylate, (b) with (methyl) acrylate of the hydroxyl of above-mentioned formula (1) expression and (c) (methyl) acrylic acid copolymer and getting, with (a) n-butyl acrylate, when (b) with (methyl) acrylate of the hydroxyl of above-mentioned formula (1) expression and (c) (methyl) acrylic acid total amount is made as 100 weight parts, (a) usage quantity of n-butyl acrylate is at 95.0～98.0 weight parts, better be in the scope of 96.0～97.5 weight parts, (b) with the usage quantity of the acrylic monomer of the hydroxyl of above-mentioned formula (1) expression at 2.0～5.0 weight parts, better be in the scope of 2.0～4.0 weight parts, and (c) (methyl) acrylic acid usage quantity below 2.0 weight parts, better be in the scope of 0.1～1.9 weight part.
As mentioned above, (A) acrylic copolymer that constitutes pressure-sensitive adhesive for optical films of the present invention is the terpolymer that is formed by the formation unit with above-mentioned formula (7-1), formula (7-2), formula (7-3) expression basically, also can be the unitary copolymer of formation that does not contain with formula (7-3) expression.In addition, can also be to have by (methyl) alkyl acrylate deutero-except that (a) n-butyl acrylate to constitute tetrapolymer or the above multiple copolymer of quaternary that the unit substitutes the unitary part of representing with formula (7-1) of formation.
In addition, (A) acrylic copolymer that uses among the present invention can have in the scope of not damaging effect of the present invention by other monomers (for example, (methyl) alkoxyalkyl acrylate, (methyl) vinylformic acid aryl ester, vinyl-acetic ester, vinyl benzene, vinylbenzene etc.) deutero-formation unit.
These (A) acrylic monomers can better be by organic solvent is made as the solution polymerization of reaction solvent among the present invention by various polymerization process polymerizations such as letex polymerization, dispersion polymerization, solution polymerizations.
(A) acrylic copolymer like this can be dissolved or dispersed in this reaction solvent the monomer that forms the aforesaid propylene acid copolymer by being reaction solvent with the organic solvent, under agitation adds polymerization starter manufacturing; Described organic solvent for example has esters solvents such as ethyl acetate, ketones solvents such as methyl ethyl ketone, formaldehyde, acetaldehyde, ether solvents such as methyl ether, aromatic series kind solvents such as toluene, dimethylbenzene, alicyclic kind solvent such as hexanaphthene, aliphatic category solvents such as hexane, octane.
As employed polymerization starter here, can exemplify 2,2 '-Diisopropyl azodicarboxylate (AIBN), 2,2 '-azo two (4-methoxyl group-2, the 4-methyl pentane nitrile), 2,2 '-azo two-2, the 4-methyl pentane nitrile, 1,1 '-azo, two hexamethylenes-azo-compounds such as 1-nitrile, the peroxidation isobutyryl, α, α '-two (new caprinoyl peroxide) diisopropyl benzene, peroxidation neodecanoic acid isopropyl benzene ester, the peroxy dicarbonate di-n-propyl ester, di-isopropyl peroxydicarbonate, peroxide-butyl carbonate, peroxidation neodecanoic acid-1,1,3,3-tetramethyl-butyl ester, peroxy dicarbonate two (4-butyl cyclohexyl ester), benzoyl peroxide, di-t-butyl peroxide, lauroyl peroxide, peroxide-2-ethyl hexanoic acid tert-butyl etc.They can be used alone or in combination.
Among the present invention, the temperature of reaction when adopting aforesaid reaction solvent and polymerization starter usually 50～90 ℃, better be that the reaction times is generally 1～10 hour, better is 2～8 hours in 60～85 ℃ the scope.
For such (A) acrylic copolymer, the weight-average molecular weight that the polystyrene standard that records by gel permeation chromatography converts better is in 1,500,000～1,850,000 scope in 1,300,000～2,000,000 scope.(A) acrylic copolymer by use has such weight-average molecular weight can form the higher tackiness agent of intensity.
Also have, the second-order transition temperature of (A) acrylic polymers of making as mentioned above is usually in-70 ℃～0 ℃ scope.
The monomeric reactivity of using when making (A) acrylic copolymer as mentioned above is good, basically with 100% reactivity polymerization, so unitary ratio of composition and monomeric feeding quantity in (A) acrylic copolymer of gained are roughly the same.
When using pressure-sensitive adhesive for optical films of the present invention, if make (B-2) linking agent that the gel fraction of (A) acrylic copolymer is reached in 65～95% the scope, better to be in 70～85% the scope, then can suppress swelling, peeling off of blooming effectively, therefore preferred.Here employed (B-2) linking agent is isocyanate compound normally.Example as spendable isocyanate compound among the present invention, can exemplify tolylene diisocyanate, tetramethylene diisocyanate, the ditan triisocyanate, the chlorobenzene vulcabond, hexamethylene diisocyanate, xylylene diisocyanate, the diphenylene methane vulcabond, diisocyanate monomer such as hydrogenated diphenyl methane diisocyanate and make TriMethylolPropane(TMP) etc. with these isocyanate-monomer additions isocyanate compound or isocyanuric acid esterification thing, biuret type compound, and make polyether glycol or polyester polyol, the acrylic acid or the like polyvalent alcohol, polybutadiene polyol, polyisoprene polyvalent alcohol etc. carry out addition reaction with them and the isocyanic ester of urethane prepolymer type.These isocyanate compounds can be used alone or in combination.Wherein, if make at least a kind of isocyanate compound being selected from tolylene diisocyanate, xylylene diisocyanate, hexamethylene diisocyanate and tetramethylene diisocyanate and TriMethylolPropane(TMP) carry out addition reaction compound carry out crosslinked, then elasticity, the intensity of the tackiness agent of gained can be adjusted in the preferred range, therefore preferred.
In order to use (B-2) linking agent of forming by such isocyanate compound that the gel fraction of tackiness agent is set in the above-mentioned scope, its usage quantity with respect to 100 weight parts (A) acrylic copolymer usually at 0.1～0.4 weight part, better be in the scope of 0.15～0.30 weight part.
By mixing isocyanate compound like this, (b) that forms (A) acrylic copolymer combines with isocyanate compound with the hydroxyl of (methyl) acrylate of the hydroxyl of above-mentioned formula (1) expression and forms crosslinking structure, the side chain of should (B-2) linking agent main and (A) acrylic copolymer form crosslinking structure with begin second several carbon atom bonded hydroxyls to combine from-CO-O-base, so can be not really up to the mark, for pressure-sensitive adhesive for optical films, demonstrate good elasticity power, and the intensity height.Also have; usually go back polymerization in (A) acrylic copolymer among the present invention (c) (methyl) vinylformic acid is arranged; this acrylic acid carboxyl of (c) (methyl) also has the reactivity with linking agent; but in fact this derives from the main chain that the acrylic acid carboxyl of (c) (methyl) approaches (A) acrylic copolymer; and (a) side chain of n-butyl acrylate forms steric hindrance; thereby react with linking agent hardly, keep the form of carboxyl.
(A) acrylic copolymer that uses in the pressure-sensitive adhesive for optical films of the present invention has following rerum natura.
(A) acrylic copolymer in being dissolved in organic solvent adds (B-1) linking agent, the condition that reaches 1mm with dried thickness is coated on the separability PET film, form coating layer, by drying remove desolvate after, lining separability PET film on the another side of this coating layer, slaking is 4～7 days under 23 ℃, the condition of 65%RH, cut out sample from the adhesive sheet of gained with the size of 5mm * 30mm * 1mm, elongation in the times of try to achieve when using described sample 90 ℃ is at (2-1) more than 1400%, and the breaking tenacity in the time of 90 ℃ is at 13～30g/mm 2Scope in (2-2), and 1000% modulus 90 ℃ the time is at 10～20g/mm 2Scope in (2-3).Also have, the gel fraction of described adhesive sheet is in 65～95% scope.
Kind as above-mentioned (B-1) linking agent, can use the linking agent with above-mentioned (B-2) linking agent identical type, usage quantity with respect to 100 weight parts (A) acrylic copolymer usually at 0.1～0.4 weight part, better be in the scope of 0.15～0.30 weight part.
That is, of the present invention comprising (A) acrylic copolymer and (B-2) linking agent pressure-sensitive adhesive for optical films by usefulness (B-2) linking agent with the crosslinked rerum natura of (A) acrylic copolymer with above-mentioned (2-1)～(2-3).
As mentioned above, comprise (A) acrylic copolymer and (B-2) pressure-sensitive adhesive for optical films of the present invention of linking agent can hardening after crosslinked with (A) acrylic copolymer with (B-2) linking agent yet, elongation in the time of 90 ℃ has 1400%～3000% high elongation rate usually more than 1400%.And although have high like this elongation, breaking tenacity is still at 13～30g/mm 2Scope in, better be at 13～20g/mm 2Scope in, have very high intensity.In addition, 1000% modulus is at 10～20g/mm 2Scope in, better be at 10～15g/mm 2Scope in.Therefore, use pressure-sensitive adhesive for optical films of the present invention and the binder layer that forms can absorb the stress that produces in the functional membrane that is attached, and the form conformability might as well, so can not peel off etc. because of the metamorphosis of the functional membrane that attached.
Bonding processing optical film of the present invention forms the binder layer that is formed by aforesaid pressure-sensitive adhesive for optical films by the surface at the functional optical film and makes.
Here, the functional optical film is meant light polarizing film, phase retardation film, electromagnetic shielding film etc.The surface of at least one side of such functional membrane is formed with the binder layer that is formed by pressure-sensitive adhesive for optical films of the present invention.
In the bonding processing optical film of the present invention, the thickness of binder layer in dry thickness usually at 10～30 μ m, better be in the scope of 15～25 μ m.As long as this binder layer is formed at a side surface of functional membrane, also can be formed at the two sides.In addition, the binder layer in the time of can also be as stacked multilayer functional membrane.
Pressure-sensitive adhesive for optical films of the present invention also can directly be coated the surface of functional membrane, but better be that coating contains by (A) acrylic copolymer and (B-2) organic solvent of the pressure-sensitive adhesive for optical films that forms of linking agent on the separability film, remove the surface that is attached at functional membrane after desolvating, slaking and form binder layer.
As spendable separability film here, can exemplify and the surface carried out PET film of peeling off processing etc.
Pressure-sensitive adhesive for optical films of the present invention or bonding processing optical film are because tackiness agent has good thermotolerance and humidity resistance, so even the long-time display unit that is pasted with functional membrane of using also is difficult for swelling, peeling off etc.In addition,, also be difficult for swelling, peeling off etc. even under high thermal environment or high hot high humidity environment, use for a long time, even and area of attachment big, also be difficult for taking place near peeling off its end, and difficultly swell peeling off of causing.In addition, the transparency of acrylic adhesives of the present invention is high, can cause transmittance to descend because of using acrylic adhesives of the present invention hardly.
In addition, the bounding force of pressure-sensitive adhesive for optical films of the present invention has reusability in the scope of 5～10N/25mm.
Pressure-sensitive adhesive for optical films of the present invention in that the crosslinked back of (A) acrylic copolymer is used separately, uses but also can mix other tackiness agents in the scope of not damaging its characteristic as mentioned above.
In addition, pressure-sensitive adhesive for optical films of the present invention can suitably add additives such as tackifier, silane coupling agent, low molecular weight propylene acids polymkeric substance, softening agent.
Add under the situation of additive, if above-mentioned (A) acrylic copolymer is made as 100 weight parts, then common addition is in the scope of 0.01～100 weight part.
Embodiment
Below, example embodiment comes pressure-sensitive adhesive for optical films and bonding processing optical film are described, but the present invention is not subjected to the qualification of these embodiment.
(evaluation method)
The mensuration of＜weight-average molecular weight 〉
Use device shown below to measure.Also have, weight-average molecular weight is tried to achieve as the weight-average molecular weight that polystyrene standard converts.
Device name: the (East ソ of TOSOH Co., Ltd one (strain)) system, HLC-8120
Post: TOSOH Co., Ltd's system, G7000HXL; 7.8mm1D 1 of * 30cm, GMHXL; 7.8mm1D 2 of * 30cm, G2500HXL; 7.8mm1D 1 of * 30cm
Sample concentration: be diluted to 1.5mg/cm with tetrahydrofuran (THF) 3Use the back.
Mobile phase solvent: tetrahydrofuran (THF)
Flow: 1.0cm 3/ minute
Column temperature: 40 ℃
＜gel fraction 〉
For gel fraction, take adhesive sheet after about 0.1g cross-linking curing to sample bottle, after adding the 30cc ethyl acetate and vibrating 4 hours, with the content of this sample bottle with the stainless steel metal mesh filter of 200 purposes, with the residue on the wire netting 100 ℃ of dryings 2 hours, measure dry weight, try to achieve by following formula.
Gel fraction (%)=(dry weight ÷ tackiness agent is taked weight) * 100
The measuring method of＜1000% modulus, breaking tenacity, elongation at break 〉
The adhesive sheet of thick 1mm is cut out 5mm * 30mm, use tensile test apparatus (the smart mechanism of Toyo Co., Ltd. is made the (East Yang Jing Machine of institute (strain)) system, Strograph R3), with draw speed 300mm/ minute, stress-strain curve when the condition of chuck spacing 10mm is obtained 90 ℃, measure 1000% modulus (stress during strain 1000%), breaking tenacity and the elongation till the fracture.
＜thermotolerance 〉
Shown in embodiment and comparative example, in the organic solvent solution that contains acrylic copolymer, add linking agent and after forming coating fluid, this coating fluid is coated on the PET of lift-off processing film with the condition that dry thickness reaches 20 μ m, (450mm * 350mm) places its slaking of 7 angels under 23 ℃, the condition of 65%RH to attach polaroid.
This blooming is attached at the surface of the non-alkali glass plate of thick 0.7mm with laminater, in 50 ℃, 5 atmospheric autoclaves, kept 20 minutes again.
The duplexer that obtains the like this condition with 120 ℃ was kept 2000 hours, estimate by the thermotolerance that unmatchful binder layer is arranged of peeling off, swelling of blooming.Mark in table 2～9 is represented following implication.Also have, the numeral of the right side record of mark is the time till note abnormalities.
Zero ... outward appearance is no abnormal
* ... outward appearance has unusually
＜humidity resistance 〉
To keep 2000 hours with 80 ℃, the condition of 90%RH with the same duplexer of the duplexer in the above-mentioned thermal test, estimate by the thermotolerance that unmatchful binder layer is arranged of peeling off, swelling of blooming.Mark in table 2～9 is represented following implication.Also have, the numeral of the right side record of mark is the time till note abnormalities.
Zero ... outward appearance is no abnormal
* ... outward appearance has unusually
(making embodiment 1)
The manufacturing of＜acrylic copolymer 1 〉
In the reaction unit that possesses stirrer, reflux exchanger, thermometer and nitrogen ingress pipe, add as the positive butyl esters of monomeric 96.5 parts by weight of acrylic acid (BA), 3 parts by weight of acrylic acid-2-hydroxy methacrylate (2HEA), 0.5 parts by weight of acrylic acid (AA) and as 100 weight part ethyl acetate of reaction solvent, add 0.1 weight part 2,2-Diisopropyl azodicarboxylate (AIBN), under stream of nitrogen gas,, make acrylic copolymer 1 in 60 ℃ of reactions of carrying out 4 hours.
The weight-average molecular weight of trying to achieve by gel permeation chromatography (GPC) for this acrylic copolymer 1 is 1,700,000.In addition, the second-order transition temperature of this acrylic copolymer 1 (Tg) is-52 ℃.
(making comparative example 1)
The manufacturing of＜acrylic copolymer 1C 〉
In making embodiment 1, except using the 3 parts by weight of acrylic acid-positive butyl ester of 4-hydroxyl (4HBA) replacement 3 parts by weight of acrylic acid-2-hydroxy methacrylate (2HEA), similarly operate, make acrylic copolymer 1C.
The weight-average molecular weight of similarly trying to achieve for this acrylic copolymer 1C is 1,730,000.In addition, the second-order transition temperature (Tg) of this acrylic copolymer 1C is-54 ℃.
(making embodiment 2)
The manufacturing of＜acrylic adhesives 2 〉
In the reaction unit that possesses stirrer, reflux exchanger, thermometer and nitrogen ingress pipe, add as the positive butyl esters of monomeric 95 parts by weight of acrylic acid (BA), 3 parts by weight of acrylic acid-2-hydroxy methacrylate (2HEA), 2.0 parts by weight of acrylic acid (AA) and as 100 weight part ethyl acetate of reaction solvent, add 0.1 weight part 2,2-Diisopropyl azodicarboxylate (AIBN), under stream of nitrogen gas,, make acrylic copolymer 2 in 60 ℃ of reactions of carrying out 4 hours.
The weight-average molecular weight of trying to achieve by gel permeation chromatography (GPC) for this acrylic copolymer 2 is 1,380,000.In addition, the second-order transition temperature of this acrylic copolymer 2 (Tg) is-51 ℃.
(making comparative example 2)
The manufacturing of＜acrylic copolymer 2C 〉
In making embodiment 2, except using the 3 parts by weight of acrylic acid-positive butyl ester of 4-hydroxyl (4HBA) replacement 3 parts by weight of acrylic acid-2-hydroxy methacrylate (2HEA), similarly operate, make acrylic copolymer 2C.
The weight-average molecular weight of similarly trying to achieve for this acrylic copolymer 2C is 1,440,000.In addition, the second-order transition temperature (Tg) of this acrylic copolymer 2C is-53 ℃.
(making embodiment 3)
The manufacturing of＜acrylic copolymer 3 〉
In the reaction unit that possesses stirrer, reflux exchanger, thermometer and nitrogen ingress pipe, add as the positive butyl esters of monomeric 97.1 parts by weight of acrylic acid (BA), 2.2 parts by weight of acrylic acid-2-hydroxy propyl ester (2HPA), 0.7 parts by weight of acrylic acid (AA) and as 100 weight part ethyl acetate of reaction solvent, add 0.1 weight part 2,2-Diisopropyl azodicarboxylate (AIBN), under stream of nitrogen gas,, make acrylic copolymer 3 in 65 ℃ of reactions of carrying out 4 hours.
The weight-average molecular weight of trying to achieve by gel permeation chromatography (GPC) for this acrylic copolymer 3 is 1,680,000.In addition, the second-order transition temperature of this acrylic copolymer 3 (Tg) is-52 ℃.
(making comparative example 3)
The manufacturing of＜acrylic copolymer 3C 〉
In making embodiment 3, except using the 2.2 parts by weight of acrylic acid-positive butyl ester of 4-hydroxyl (4HBA) replacement 2.2 parts by weight of acrylic acid-2-hydroxy propyl ester (2HPA), similarly operate, make acrylic copolymer 3C.
The weight-average molecular weight of similarly trying to achieve for this acrylic copolymer 3C is 1,700,000.In addition, the second-order transition temperature (Tg) of this acrylic copolymer 3C is-54 ℃.
(making embodiment 4)
The manufacturing of＜acrylic copolymer 4 〉
In the reaction unit that possesses stirrer, reflux exchanger, thermometer and nitrogen ingress pipe, add as the positive butyl esters of monomeric 71.5 parts by weight of acrylic acid (BA), 25 parts by weight of acrylic acid methyl esters (MA), 3 parts by weight of acrylic acid-2-hydroxy propyl ester (2HPA), 0.5 parts by weight of acrylic acid (AA) and as 100 weight part ethyl acetate of reaction solvent, add 0.1 weight part 2,2-Diisopropyl azodicarboxylate (AIBN), under stream of nitrogen gas,, make acrylic copolymer 4 in 60 ℃ of reactions of carrying out 4 hours.
The weight-average molecular weight of trying to achieve by gel permeation chromatography (GPC) for this acrylic copolymer 4 is 1,740,000.In addition, the second-order transition temperature of this acrylic copolymer 4 (Tg) is-39 ℃.
(making comparative example 4)
The manufacturing of＜acrylic copolymer 4C 〉
In making embodiment 4, except using the 3 parts by weight of acrylic acid-positive butyl ester of 4-hydroxyl (4HBA) replacement 3 parts by weight of acrylic acid-2-hydroxy propyl ester (2HPA), similarly operate, make acrylic copolymer 4C.
The weight-average molecular weight of similarly trying to achieve for this acrylic copolymer 4C is 1,790,000.In addition, the second-order transition temperature (Tg) of this acrylic copolymer 4C is-41 ℃.
(making embodiment 5)
The manufacturing of＜acrylic copolymer 5 〉
In the reaction unit that possesses stirrer, reflux exchanger, thermometer and nitrogen ingress pipe, add as the positive butyl esters of monomeric 96.0 parts by weight of acrylic acid (BA), 4.0 parts by weight of acrylic acid-2-hydroxy propyl ester (2HPA) and as 100 weight part ethyl acetate of reaction solvent, add 0.1 weight part 2,2-Diisopropyl azodicarboxylate (AIBN), under stream of nitrogen gas,, make acrylic copolymer 5 in 65 ℃ of reactions of carrying out 4 hours.
The weight-average molecular weight of trying to achieve by gel permeation chromatography (GPC) for this acrylic copolymer 5 is 1,700,000.In addition, the second-order transition temperature of this acrylic copolymer 5 (Tg) is-52 ℃.
(making comparative example 5)
The manufacturing of＜acrylic copolymer 5C 〉
In making embodiment 5, except using 4.0 parts by weight of acrylic acid-3-hydroxy propyl ester (3HPA) replacement 4.0 parts by weight of acrylic acid-2-hydroxy propyl ester (2HPA), similarly operate, make acrylic copolymer 5C.
The weight-average molecular weight of similarly trying to achieve for this acrylic copolymer 5C is 1,720,000.In addition, the second-order transition temperature (Tg) of this acrylic copolymer 5C is-55 ℃.
(making embodiment 6)
The manufacturing of＜acrylic copolymer 6 〉
To possessing stirrer, reflux exchanger, add in the reaction unit of thermometer and nitrogen ingress pipe as the positive butyl esters of monomeric 96.7 parts by weight of acrylic acid (BA), 2.6 parts by weight of acrylic acid-2-hydroxy methacrylate (2HEA), 0.7 parts by weight of acrylic acid (AA) and be the vinyl-acetic ester (Vac) of 2 weight parts and as 100 weight part ethyl acetate of reaction solvent with respect to above-mentioned (BA)+(2HEA)+(AA)=100 weight part, add 0.1 weight part 2,2-Diisopropyl azodicarboxylate (AIBN), under stream of nitrogen gas,, make acrylic copolymer 6 in 60 ℃ of reactions of carrying out 4 hours.
The weight-average molecular weight of trying to achieve by gel permeation chromatography (GPC) for this acrylic copolymer 6 is 1,600,000.In addition, the second-order transition temperature of this acrylic copolymer 6 (Tg) is-54 ℃.
(making comparative example 6)
The manufacturing of＜acrylic copolymer 6C 〉
In making embodiment 6, except using the 2.6 parts by weight of acrylic acid-positive butyl ester of 4-hydroxyl (4HBA) replacement 2.6 parts by weight of acrylic acid-2-hydroxy methacrylate (2HEA), similarly operate, make acrylic copolymer 6C.
The weight-average molecular weight of similarly trying to achieve for this acrylic copolymer 6C is 1,620,000.In addition, the second-order transition temperature (Tg) of this acrylic copolymer 6C is-56 ℃.
(making embodiment 7)
The manufacturing of＜acrylic copolymer 7 〉
In the reaction unit that possesses stirrer, reflux exchanger, thermometer and nitrogen ingress pipe, add as the positive butyl esters of monomeric 95.7 parts by weight of acrylic acid (BA), 2.6 parts by weight of acrylic acid-2-hydroxy methacrylate (2HEA), 1.4 parts by weight of acrylic acid-2-hydroxy propyl ester (2HPA), 0.3 parts by weight of acrylic acid (AA) and as 100 weight part ethyl acetate of reaction solvent, add 0.1 weight part 2,2-Diisopropyl azodicarboxylate (AIBN), under stream of nitrogen gas,, make acrylic copolymer 7 in 60 ℃ of reactions of carrying out 4 hours.
The weight-average molecular weight of trying to achieve by gel permeation chromatography (GPC) for this acrylic copolymer 7 is 1,810,000.In addition, the second-order transition temperature of this acrylic copolymer 7 (Tg) is-52 ℃.
(making comparative example 7)
The manufacturing of＜acrylic copolymer 7C 〉
In making embodiment 7, except using the 4 parts by weight of acrylic acid-positive butyl ester of 4-hydroxyl (4HBA) replacement 2.6 parts by weight of acrylic acid-2-hydroxy methacrylate (2HEA), 1.4 parts by weight of acrylic acid-2-hydroxy propyl ester (2HPA), similarly operate, make acrylic copolymer 7C.
The weight-average molecular weight of similarly trying to achieve for this acrylic copolymer 7C is 1,880,000.In addition, the second-order transition temperature (Tg) of this acrylic copolymer 7C is-55 ℃.
Acrylic copolymer of making as mentioned above 1～7 and the composition transitivity of acrylic copolymer 1C～7C are shown in table 1.
(making comparative example 8)
The manufacturing of＜acrylic adhesives 8C 〉
In the reaction unit that possesses stirrer, reflux exchanger, thermometer and nitrogen ingress pipe, add as the positive butyl esters of monomeric 92.5 parts by weight of acrylic acid (BA), 7 parts by weight of acrylic acid-2-hydroxy methacrylate (2HEA), 0.5 parts by weight of acrylic acid (AA) and as 100 weight part ethyl acetate of reaction solvent, add 0.1 weight part 2,2-Diisopropyl azodicarboxylate (AIBN), under stream of nitrogen gas,, make acrylic adhesives 8C in 60 ℃ of reactions of carrying out 4 hours.
The weight-average molecular weight of trying to achieve by gel permeation chromatography (GPC) for this acrylic adhesives 8C is 1,880,000.In addition, the second-order transition temperature (Tg) of this acrylic adhesives 8C is-51 ℃.
(making comparative example 9)
The manufacturing of＜acrylic adhesives 9C 〉
In the reaction unit that possesses stirrer, reflux exchanger, thermometer and nitrogen ingress pipe, add as the positive butyl esters of monomeric 98.5 parts by weight of acrylic acid (BA), 1 parts by weight of acrylic acid-2-hydroxy methacrylate (2HEA), 0.5 parts by weight of acrylic acid (AA) and as 100 weight part ethyl acetate of reaction solvent, add 0.1 weight part 2,2-Diisopropyl azodicarboxylate (AIBN), under stream of nitrogen gas,, make acrylic adhesives 9C in 60 ℃ of reactions of carrying out 4 hours.
The weight-average molecular weight of trying to achieve by gel permeation chromatography (GPC) for this acrylic adhesives 9C is 1,640,000.In addition, the second-order transition temperature (Tg) of this acrylic adhesives 9C is-53 ℃.
(making comparative example 10)
The manufacturing of＜acrylic adhesives 10C 〉
In the reaction unit that possesses stirrer, reflux exchanger, thermometer and nitrogen ingress pipe, add as the positive butyl esters of monomeric 96.5 parts by weight of acrylic acid (BA), 3 parts by weight of acrylic acid-2-hydroxy methacrylate (2HEA), 0.5 parts by weight of acrylic acid (AA) and as 130 weight part ethyl acetate of reaction solvent, add 0.1 weight part 2,2-Diisopropyl azodicarboxylate (AIBN), under stream of nitrogen gas,, make acrylic adhesives 10C in 65 ℃ of reactions of carrying out 4 hours.
The weight-average molecular weight of trying to achieve by gel permeation chromatography (GPC) for this acrylic adhesives 10C is 1,210,000.In addition, the second-order transition temperature (Tg) of this acrylic adhesives 10C is-53 ℃.
(making comparative example 11)
The manufacturing of＜acrylic adhesives 11C 〉
In the reaction unit that possesses stirrer, reflux exchanger, thermometer and nitrogen ingress pipe, add as the positive butyl esters of monomeric 94 parts by weight of acrylic acid (BA), 6 parts by weight of acrylic acid (AA) and as 90 weight part ethyl acetate of reaction solvent, add 0.1 weight part 2,2-Diisopropyl azodicarboxylate (AIBN), under stream of nitrogen gas,, make acrylic adhesives 11C in 60 ℃ of reactions of carrying out 4 hours.
The weight-average molecular weight of trying to achieve by gel permeation chromatography (GPC) for this acrylic adhesives 11C is 1,820,000.In addition, the second-order transition temperature (Tg) of this acrylic adhesives 11C is-48 ℃.
Table 1
Acrylic copolymer ??BA ??MA ??2HEA ??2HPA ??3HPA ??4HBA ??AA ??Vac ??Mw ??Tg(℃)
Acrylic copolymer 1 ??96.5 ??3 ??0.5 1,700,000 ??-52
Acrylic copolymer 1C ??96.5 ??3 ??0.5 1,730,000 ??-54
Acrylic copolymer 2 ??95 ??3 ??2 1,380,000 ??-51
Acrylic copolymer 2C ??95 ??3 ??2 1,440,000 ??-53
Acrylic copolymer 3 ??97.1 ??2.2 ??0.7 1,680,000 ??-52
Acrylic copolymer 3C ??97.1 ??2.2 ??0.7 1,700,000 ??-54
Acrylic copolymer 4 ??71.5 ??25 ??3 ??0.5 1,740,000 ??-39
Acrylic copolymer 4C ??71.5 ??25 ??3 ??0.5 1,790,000 ??-41
Acrylic copolymer 5 ??96 ??4 1,700,000 ??-52
Acrylic copolymer 5C ??96 ??4 1,720,000 ??-55
Acrylic copolymer 6 ??96.7 ??2.6 ??0.7 ??2 1,600,000 ??-54
Acrylic copolymer 6C ??96.7 ??2.6 ??0.7 ??2 1,620,000 ??-56
Acrylic copolymer 7 ??95.7 ??2.6 ??1.4 ??0.3 1,810,000 ??-52
Acrylic copolymer 7C ??95.7 ??4 ??0.3 1,880,000 ??-55
Acrylic copolymer 8C ??92.5 ??7 ??0.5 1,880,000 ??-51
Acrylic copolymer 9C ??98.5 ??1 ??0.5 1,640,000 ??-53
Acrylic copolymer 10C ??96.5 ??3 ??0.5 1,210,000 ??-53
Acrylic copolymer 11C ??94 ??6 1,820,000 ??-48
Notes) in the table 1,
BA is a n-butyl acrylate,
MA is a methyl acrylate,
2HEA is a 2-Hydroxy ethyl acrylate,
2HPA is vinylformic acid-2-hydroxy propyl ester,
3HPA is vinylformic acid-3-hydroxy propyl ester,
4HBA is vinylformic acid-positive butyl ester of 4-hydroxyl,
AA is a vinylformic acid,
Vac is a vinyl-acetic ester.
(embodiment 1)
Mix 0.2 weight part KBE-9007 (Shin-Etsu Polymer Co., Ltd's (the Port リ マ of SHIN-ETSU HANTOTAI one (strain)) system in the acrylic copolymer of in 100 weight parts manufacturing embodiment 1, making 1, isocyanate-based silane coupling agent) and 0.2 weight part isocyanates linking agent (CORONATE L: Nippon Polyurethane Industry Co., Ltd.'s (Japanese Port リ ウ レ タ Application (strain)) system), hydroxyl in the acrylic copolymer is reacted with the isocyanates linking agent and make pressure-sensitive adhesive for optical films.
Its coating fluid is coated through the surface of the PET of lift-off processing film with the condition that dry thickness reaches 20 μ m, removed and to desolvate, be attached at polaroid, under 23 ℃, the condition of 65%HR, make its slaking 7 days, thereby obtain bonding processing optical film.
In addition, its coating fluid is coated through the surface of the PET of lift-off processing film with the condition that dry thickness reaches 1mm, removed and to desolvate, be attached at another, under 23 ℃, the condition of 65%HR, make its slaking 7 days, thereby obtain adhesive sheet through the PET of lift-off processing film.
The gel fraction of this adhesive sheet is 75%.
By above-mentioned method the characteristic of the pressure-sensitive adhesive for optical films of gained, bonding processing optical film and adhesive sheet is investigated.The results are shown in table 2.
(comparative example 1)
Among the embodiment 1, the acrylic copolymer 1C that makes in using manufacturing comparative example 1 replaces making acrylic copolymer of making among the embodiment 11 and the amount that changes CORONATE L, similarly operate, make pressure-sensitive adhesive for optical films, bonding processing optical film and adhesive sheet, their characteristic is investigated by above-mentioned method.The result is shown in table 2 in the lump.
Table 2
Figure G2008800072290D00261
(embodiment 2)
Mix 0.2 weight part isocyanates linking agent (CORONATE L: Nippon Polyurethane Industry Co., Ltd.'s system), hydroxyl in the acrylic copolymer is reacted with the isocyanates linking agent and make pressure-sensitive adhesive for optical films in the acrylic copolymer of in 100 weight parts are made embodiment 2, making 2.
Its coating fluid is coated through the surface of the PET of lift-off processing film with the condition that dry thickness reaches 20 μ m, removed and to desolvate, be attached at polaroid, under 23 ℃, the condition of 65%HR, make its slaking 7 days, thereby obtain bonding processing optical film.
In addition, its coating fluid is coated through the surface of the PET of lift-off processing film with the condition that dry thickness reaches 1mm, removed and to desolvate, be attached at another, under 23 ℃, the condition of 65%HR, make its slaking 7 days, thereby obtain adhesive sheet through the PET of lift-off processing film.
The gel fraction of this adhesive sheet is 82%.
By above-mentioned method the characteristic of the pressure-sensitive adhesive for optical films of gained, bonding processing optical film and adhesive sheet is investigated.The results are shown in table 3.
(comparative example 2)
Among the embodiment 2, the acrylic copolymer 2C that makes in using manufacturing comparative example 2 replaces making acrylic copolymer of making among the embodiment 22 and the amount that changes CORONATE L, similarly operate, make pressure-sensitive adhesive for optical films, bonding processing optical film and adhesive sheet, their characteristic is investigated by above-mentioned method.The result is shown in table 3 in the lump.
Table 3
Figure G2008800072290D00271
(embodiment 3)
Mix 0.25 weight part isocyanates linking agent (CORONATE L: Nippon Polyurethane Industry Co., Ltd.'s system), hydroxyl in the acrylic copolymer is reacted with the isocyanates linking agent and make pressure-sensitive adhesive for optical films in the acrylic copolymer of in 100 weight parts are made embodiment 3, making 3.
Its coating fluid is coated through the surface of the PET of lift-off processing film with the condition that dry thickness reaches 20 μ m, removed and to desolvate, be attached at polaroid, under 23 ℃, the condition of 65%HR, make its slaking 7 days, thereby obtain bonding processing optical film.
In addition, its coating fluid is coated through the surface of the PET of lift-off processing film with the condition that dry thickness reaches 1mm, removed and to desolvate, be attached at another, under 23 ℃, the condition of 65%HR, make its slaking 7 days, thereby obtain adhesive sheet through the PET of lift-off processing film.
The gel fraction of this adhesive sheet is 81%.
By above-mentioned method the characteristic of the pressure-sensitive adhesive for optical films of gained, bonding processing optical film and adhesive sheet is investigated.The results are shown in table 4.
(comparative example 3)
Among the embodiment 3, the acrylic copolymer 3C that makes in using manufacturing comparative example 3 replaces making acrylic copolymer of making among the embodiment 33 and the amount that changes CORONATE L, similarly operate, make pressure-sensitive adhesive for optical films, bonding processing optical film and adhesive sheet, their characteristic is investigated by above-mentioned method.The result is shown in table 4 in the lump.
Table 4
Figure G2008800072290D00281
(embodiment 4)
Mix 0.2 weight part isocyanates linking agent (CORONATE L: Nippon Polyurethane Industry Co., Ltd.'s system), hydroxyl in the acrylic copolymer is reacted with the isocyanates linking agent and make pressure-sensitive adhesive for optical films in the acrylic copolymer of in 100 weight parts are made embodiment 4, making 4.
Its coating fluid is coated through the surface of the PET of lift-off processing film with the condition that dry thickness reaches 20 μ m, removed and to desolvate, be attached at polaroid, under 23 ℃, the condition of 65%HR, make its slaking 7 days, thereby obtain bonding processing optical film.
In addition, its coating fluid is coated through the surface of the PET of lift-off processing film with the condition that dry thickness reaches 1mm, removed and to desolvate, be attached at another, under 23 ℃, the condition of 65%HR, make its slaking 7 days, thereby obtain adhesive sheet through the PET of lift-off processing film.
The gel fraction of this adhesive sheet is 75%.
By above-mentioned method the characteristic of the pressure-sensitive adhesive for optical films of gained, bonding processing optical film and adhesive sheet is investigated.The results are shown in table 5.
(comparative example 4)
Among the embodiment 4, the acrylic copolymer 4C that makes in using manufacturing comparative example 4 replaces making acrylic copolymer of making among the embodiment 44 and the amount that changes CORONATE L, similarly operate, make pressure-sensitive adhesive for optical films, bonding processing optical film and adhesive sheet, their characteristic is investigated by above-mentioned method.The result is shown in table 5 in the lump.
Table 5
Figure G2008800072290D00291
(embodiment 5)
Mix 0.3 weight part isocyanates linking agent (CORONATE L: Nippon Polyurethane Industry Co., Ltd.'s system), hydroxyl in the acrylic copolymer is reacted with the isocyanates linking agent and make pressure-sensitive adhesive for optical films in the acrylic copolymer of in 100 weight parts are made embodiment 5, making 5.
Its coating fluid is coated through the surface of the PET of lift-off processing film with the condition that dry thickness reaches 20 μ m, removed and to desolvate, be attached at polaroid, under 23 ℃, the condition of 65%HR, make its slaking 7 days, thereby obtain bonding processing optical film.
In addition, its coating fluid is coated through the surface of the PET of lift-off processing film with the condition that dry thickness reaches 1mm, removed and to desolvate, be attached at another, under 23 ℃, the condition of 65%HR, make its slaking 7 days, thereby obtain adhesive sheet through the PET of lift-off processing film.
The gel fraction of this adhesive sheet is 78%.
By above-mentioned method the characteristic of the pressure-sensitive adhesive for optical films of gained, bonding processing optical film and adhesive sheet is investigated.The results are shown in table 6.
(comparative example 5)
Among the embodiment 5, the acrylic copolymer 5C that makes in using manufacturing comparative example 5 replaces making acrylic copolymer of making among the embodiment 55 and the amount that changes CORONATE L, similarly operate, make pressure-sensitive adhesive for optical films, bonding processing optical film and adhesive sheet, their characteristic is investigated by above-mentioned method.The result is shown in table 6 in the lump.
Table 6
Figure G2008800072290D00301
(embodiment 6)
Mix 0.25 weight part isocyanates linking agent (CORONATE L: Nippon Polyurethane Industry Co., Ltd.'s system), hydroxyl in the acrylic copolymer is reacted with the isocyanates linking agent and make pressure-sensitive adhesive for optical films in the acrylic copolymer of in 100 weight parts are made embodiment 6, making 6.
Its coating fluid is coated through the surface of the PET of lift-off processing film with the condition that dry thickness reaches 20 μ m, removed and to desolvate, be attached at polaroid, under 23 ℃, the condition of 65%HR, make its slaking 7 days, thereby obtain bonding processing optical film.
In addition, its coating fluid is coated through the surface of the PET of lift-off processing film with the condition that dry thickness reaches 1mm, removed and to desolvate, be attached at another, under 23 ℃, the condition of 65%HR, make its slaking 7 days, thereby obtain adhesive sheet through the PET of lift-off processing film.
The gel fraction of this adhesive sheet is 78%.
By above-mentioned method the characteristic of the pressure-sensitive adhesive for optical films of gained, bonding processing optical film and adhesive sheet is investigated.The results are shown in table 7.
(comparative example 6)
Among the embodiment 6, the acrylic copolymer 6C that makes in using manufacturing comparative example 6 replaces making acrylic copolymer of making among the embodiment 66 and the amount that changes CORONATE L, similarly operate, make pressure-sensitive adhesive for optical films, bonding processing optical film and adhesive sheet, their characteristic is investigated by above-mentioned method.The result is shown in table 7 in the lump.
Table 7
Figure G2008800072290D00311
(embodiment 7)
Mix 0.15 weight part isocyanates linking agent (CORONATE L: Nippon Polyurethane Industry Co., Ltd.'s system), hydroxyl in the acrylic copolymer is reacted with the isocyanates linking agent and make pressure-sensitive adhesive for optical films in the acrylic copolymer of in 100 weight parts are made embodiment 7, making 7.
Its coating fluid is coated through the surface of the PET of lift-off processing film with the condition that dry thickness reaches 20 μ m, removed and to desolvate, be attached at polaroid, under 23 ℃, the condition of 65%HR, make its slaking 7 days, thereby obtain bonding processing optical film.
In addition, its coating fluid is coated through the surface of the PET of lift-off processing film with the condition that dry thickness reaches 1mm, removed and to desolvate, be attached at another, under 23 ℃, the condition of 65%HR, make its slaking 7 days, thereby obtain adhesive sheet through the PET of lift-off processing film.
The gel fraction of this adhesive sheet is 78%.
By above-mentioned method the characteristic of the pressure-sensitive adhesive for optical films of gained, bonding processing optical film and adhesive sheet is investigated.The results are shown in table 8.
(comparative example 7)
Among the embodiment 7, the acrylic copolymer 7C that makes in using manufacturing comparative example 7 replaces making acrylic copolymer of making among the embodiment 77 and the amount that changes CORONATE L, similarly operate, make pressure-sensitive adhesive for optical films, bonding processing optical film and adhesive sheet, their characteristic is investigated by above-mentioned method.The result is shown in table 8 in the lump.
Table 8
Figure G2008800072290D00321
(comparative example 8～11)
Acrylic copolymer 8C～11C that in using above-mentioned manufacturing comparative example 8～11, makes and the amount that changes CORONATE L, operate similarly to Example 1, make the blooming acrylic adhesives, re-use this tackiness agent and make bonding processing optical film as mentioned above.
For pressure-sensitive adhesive for optical films, processing optical film and the adhesive sheet of gained, similarly estimate with the foregoing description 1, fail to obtain good result.
The result gathers and is shown in table 9.
Table 9
The possibility of utilizing on the industry
As mentioned above, pressure-sensitive adhesive for optical films of the present invention or bonding processing optical film are by the composition of adjusting (A) acrylic copolymer, the formation state of cross-linked structure etc., add crosslinking agent in this adhesive and percentage elongation during 90 ℃ of acrylic adhesives layer when forming adhesive phase reaches more than 1400%, fracture strength reaches 13g/mm2More than, and 1000% modulus reaches 10g/mm2More than. And not only balance is good and have good elasticity as mentioned above for pressure-sensitive adhesive for optical films of the present invention or bonding processing optical film, and is also good aspect the optical characteristics that represents with total light transmittance or mist degree.
Therefore, adhesive of the present invention is when being used as the adhesive of blooming, demonstrate in the nature of things good heat resistance, humidity resistance is also good, even the adhesive during as films such as attaching polarizer, polarizers in liquid crystal indicator, PDP display unit etc., internal stress etc. also are absorbed by acrylic adhesives, difficultly peel off, swell etc.
In addition, come in the situation of cling film with bonding sheet or adhesive with blooming of the present invention, even there is the stickup of film to damage, also can easily adhesive be peeled off to carry out re-posted from clung body. And, be difficult for the characteristic at the surface of clung body generation cull when also having such re-posted.

Claims (9)

1. a pressure-sensitive adhesive for optical films is characterized in that, comprise with
(a) n-butyl acrylate 95.0～98.0 weight parts,
(b) with (methyl) acrylate 2.0～5.0 weight parts of the hydroxyl of following formula (1) expression and
(c) the following amount copolymerization of (methyl) vinylformic acid 2.0 weight parts and
(A) acrylic copolymer, and satisfy following condition (1)～(3), the summation of above-mentioned (a)～(c) is 100 weight parts;
Condition (1): (A) acrylic copolymer passes through weight-average molecular weight that polystyrene standard that gel permeation chromatography records converts in 1,300,000～2,000,000 scope;
Condition (2): (A) acrylic copolymer in being dissolved in organic solvent adds (B-1) linking agent, the condition that reaches 1mm with dried thickness is coated on the separability PET film, form coating layer, by drying remove desolvate after, lining separability PET film on the another side of this coating layer, slaking is 4～7 days under 23 ℃, the condition of 65%RH, cut out sample from the adhesive sheet of gained with the size of 5mm * 30mm * 1mm, elongation in the times of try to achieve when using described sample 90 ℃ is at (2-1) more than 1400%, and the breaking tenacity in the time of 90 ℃ is at 13～30g/mm 2Scope in (2-2), and 1000% modulus 90 ℃ the time is at 10～20g/mm 2Scope in (2-3);
Condition (3): the gel fraction of described adhesive sheet is in 65～95% scope;
Figure A2008800072290002C1
In the above-mentioned formula (1), R 1Expression hydrogen atom or methyl, R 2The alkyl of expression hydrogen atom or carbon number 1～2.
2. a pressure-sensitive adhesive for optical films is characterized in that, comprise with
(a) n-butyl acrylate 95.0～98.0 weight parts,
(b) with (methyl) acrylate 2.0～5.0 weight parts of the hydroxyl of following formula (1) expression and
(c) the following amount copolymerization of (methyl) vinylformic acid 2.0 weight parts and
(A) acrylic copolymer and
(B-2) linking agent, and satisfy following condition (1)～(3), the summation of above-mentioned (a)～(c) is 100 weight parts;
Condition (1): (A) acrylic copolymer passes through weight-average molecular weight that polystyrene standard that gel permeation chromatography records converts in 1,300,000～2,000,000 scope;
Condition (2): (A) acrylic copolymer in being dissolved in organic solvent adds (B-1) linking agent, the condition that reaches 1mm with dried thickness is coated on the separability PET film, form coating layer, by drying remove desolvate after, lining separability PET film on the another side of this coating layer, slaking is 4～7 days under 23 ℃, the condition of 65%RH, cut out sample from the adhesive sheet of gained with the size of 5mm * 30mm * 1mm, elongation in the times of try to achieve when using described sample 90 ℃ is at (2-1) more than 1400%, and the breaking tenacity in the time of 90 ℃ is at 13～30g/mm 2Scope in (2-2), and 1000% modulus 90 ℃ the time is at 10～20g/mm 2Scope in (2-3);
Condition (3): the gel fraction of described adhesive sheet is in 65～95% scope;
Figure A2008800072290003C1
In the above-mentioned formula (1), R 1Expression hydrogen atom or methyl, R 2The alkyl of expression hydrogen atom or carbon number 1～2.
3. pressure-sensitive adhesive for optical films as claimed in claim 1 or 2 is characterized in that, in the condition (2), if (A) acrylic copolymer is made as 100 weight parts, then (B-1) linking agent is 0.1～0.4 weight part.
4. pressure-sensitive adhesive for optical films as claimed in claim 2 is characterized in that, if (A) acrylic copolymer contained in the pressure-sensitive adhesive for optical films is made as 100 weight parts, then (B-2) linking agent is 0.1～0.4 weight part.
5. as each the described pressure-sensitive adhesive for optical films in the claim 1～4, it is characterized in that (B-1) linking agent is an isocyanate compound.
6. pressure-sensitive adhesive for optical films as claimed in claim 2 is characterized in that (B-2) linking agent is an isocyanate compound.
7. as each the described pressure-sensitive adhesive for optical films in the claim 1～6, it is characterized in that described (A) acrylic copolymer is a terpolymer.
8. as each the described pressure-sensitive adhesive for optical films in the claim 1～6, it is characterized in that the part of described (a) n-butyl acrylate is replaced by (methyl) alkyl acrylate except that n-butyl acrylate.
9. a bonding processing optical film is characterized in that, comprising:
The functional optical film and
The binder layer that on the functional optical film, forms by following pressure-sensitive adhesive for optical films;
Described pressure-sensitive adhesive for optical films comprise with
(a) n-butyl acrylate 95.0～98.0 weight parts,
(b) with (methyl) acrylate 2.0～5.0 weight parts of the hydroxyl of following formula (1) expression and
(c) the following amount copolymerization of (methyl) vinylformic acid 2.0 weight parts and
(A) acrylic copolymer and
(B-2) linking agent, and satisfy following condition (1)～(3), the summation of above-mentioned (a)～(c) is 100 weight parts;
Condition (1): (A) acrylic copolymer passes through weight-average molecular weight that polystyrene standard that gel permeation chromatography records converts in 1,300,000～2,000,000 scope;
Condition (2): (A) acrylic copolymer in being dissolved in organic solvent adds (B-1) linking agent, the condition that reaches 1mm with dried thickness is coated on the separability PET film, form coating layer, by drying remove desolvate after, lining separability PET film on the another side of this coating layer, slaking is 4～7 days under 23 ℃, the condition of 65%RH, cut out sample from the adhesive sheet of gained with the size of 5mm * 30mm * 1mm, elongation in the times of try to achieve when using described sample 90 ℃ is at (2-1) more than 1400%, and the breaking tenacity in the time of 90 ℃ is at 13～30g/mm 2Scope in (2-2), and 1000% modulus 90 ℃ the time is at 10～20g/mm 2Scope in (2-3);
Condition (3): the gel fraction of described adhesive sheet is in 65～95% scope;
Figure A2008800072290005C1
In the above-mentioned formula (1), R 1Expression hydrogen atom or methyl, R 2The alkyl of expression hydrogen atom or carbon number 1～2.
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